Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Turkey (TR-ROP study): a prospective, multicentre study in 69 neonatal

Autor: Bas, AY, Demirel, N, Koc, E, Isik, DU, Hirfanoglu, IM, Tunc, T, Sari, FN, Karatekin, G, Koklu, E, Altunhan, H, Turgut, H, Narter, F, Tarakci, N, Tekgunduz, KS, Ozkiraz, S, Aydemir, C, Ozdemir, A, Cetinkaya, B, Kazanci, E, Tastekin, A, Calkavur, S, Ozyurt, BM, Demirelli, Y, Asker, HS, Mutlu, B, Uygur, O, Ozkan, H, Armangil, D, Ozlu, F, Mert, MK, Ergin, H, Ozcan, B, Bas, EK, Okulu, E, Acunas, B, Celik, U, Uslu, SI, Mutlu, M, Demir, N, Eroglu, F, Gokmen, Z, Beken, S, Bayraktar, BT, Hakan, N, Kucuktasci, K, Orman, A, Comert, S, Ertugrul, S, Ustun, N, Sahin, O, Terek, D, Kale, Y, Konak, M, Yurttutan, S, Aydemir, O, Zenciroglu, A, Sarici, D, Guzoglu, N, Hamilcikan, S, Gursoy, T, Tuzun, F, Ors, R, Arslan, S, Akdag, A, Memisoglu, A, Yasa, B, Hekimoglu, B, Turan, O, Aylanc, H, Takci, S, Celik, T, Sahin, S, Kilic, I, Kara, C, Tunay, ZO, Celik, G, Gozen, I, Satirtav, G, Polat, N, Oral, AY, Tokgoz, M, Keles, S, Bilgin, B, Ugurbas, SC, Karaca, C, Keskek, NS, Ekinci, DY, Balci, O, Altan, EV, Bakbak, S, Ceylan, NA, Kimyon, S, Alyamac, G, Ture, G, Yildiz, M, Calis, F, Sizmaz, S, Sukgen, E, Cetin, EN, Ozcimen, M, Demir, ST, Atila, H, Ozal, A, Tufaner, G, Yucel, OE, Kola, M, Seven, E, Ozdek, S, Durukan, AH, Kal, A, Celebi, ARC, Koytak, IA, Alacamli, G, Esme, A, Catak, O, Perente, I, Sahin, A, Akcakaya, AA, Kiray, G, Nalcaci, S, Aksoy, U, Bakbak, B, Comez, A, Gursoy, H, Kabatas, EU, Petricli, IS, Yumusak, ME, Kirgiz, A, Uludag, G, Yaman, A, Dadaci, Z, Karatas, A, Celiker, H, Cebeci, Z, Esenulku, MC, Akkoyun, I, Ersan, I, Demir, S, Kadayifcilar, S, Unsal, AIA, Hocaoglu, M

Background To evaluate the prevalence, risk factors and treatment of retinopathy of prematurity (ROP) in Turkey and to establish screening criteria for this condition. Methods A prospective cohort study (TR-ROP) was performed between 1 April 2016 and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::9390d142adea37d0642300b929239bf0
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/16237

Fatal pulmonary embolism due to ınherited thrombophilia factors in a child with wolfram syndrome

Autor: Kucuktasci, K., Semiz, Serap, Balcı, Yasemin Işık, Özsari, T., Gürses, Dolunay, Önem, Gökhan, Saçar, Mustafa, Düzcan, Füsun, Yüksel, Doğangün, Semiz, Ender

Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus (DM), optic atrophy, diabetes insipidus, and deafness. Poorly controlled type 1 DM increases the risk for thrombosis. However, co

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3566::95ebf7febbc875e0c074fbc38f2d4243
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/9422

Risk factors of newborns with periventricular/intraventricular hemorrhage

Autor: Özdemir, Özmert Muhammet Ali, Gürses, Merve, Kucuktasci, K, Kocyigit, A, Ergin, Hacer

Objective: Periventricular/intraventricular hemorrhage (PV/IVH) is the most common type of intracranial hemorrhage in the neonatal period. PV/IVH may cause significant neurodevelopmental problems for preterms, even it can be fatal. Low-birth weight a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3351d866f464c89158e0369b424b6000
https://hdl.handle.net/11499/22200

Neonatal Bartter Syndrome: A Newborn Case

Autor: Ozdemir, OMA, Kucuktasci, K, Ozdemir, E, Urey, T, Ergin, H, Evrengul, H

Neonatal Bartter syndrome (BS) is an inherited renal tubular disorder characterized with normal blood pressure, hypokalemia, hypochloremic metabolic alkalosis, hyperreninemia and increased urinary loss of sodium, potassium and chloride. In this disor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f79c1dd84d81a71337e76baa93c81611
https://doi.org/10.4274/jpr.14633